Circularly polarized multiple-resonance
thermally activated delayed
fluorescence (CP-MR-TADF) materials have received widespread attention
in recent years, but it remains a formidable challenge to design high-performance
CP-MR-TADF emitters concurrently exhibiting high quantum efficiency,
narrowband emission, and high dissymmetry factor (g). Here, we perform an in-depth theoretical investigation on the
CP-MR-TADF materials based on [2.2] paracyclophane (pCp) derivatives.
The MR-based materials with enhanced long-range charge transfer (LRCT)
characteristics upon excitation show increased g values
owing to the coaxial dominated transition components of the transition
electric dipole moment (TEDM) and the transition magnetic dipole moment
(TMDM) but inevitably result in the loss of narrowband emission performance.
Furthermore, the newly designed molecules by fusing the peripheral
benzene units of MR cores within the planar chiral pCp bridge maintain
narrowband emissions and exhibit increased g values
on the order of 1 × 10–3. These findings with
rich physical insights on the structure–performance relation
of chiral paracyclophane-based molecules should provide important
clues for designing high-performance chiral materials.